COPS6 COP9 signalosome subunit 6

Information
Symbol
COPS6
Type
protein-coding
Description
COP9 signalosome subunit 6
Entrez Gene ID
10980
Genome
hg19
Position
chr7:99,686,592-99,689,810
Genome
hg38
Position
chr7:100,088,969-100,092,187
MIM
614729 OMIM
HGNC
HGNC:21749 HGNC
Ensembl
ENSG00000168090 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
18
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CSN6
SYNONYM MOV34-34KD
MIM 614729 OMIM
HGNC HGNC:21749 HGNC
Ensembl ENSG00000168090 Ensembl
AllianceGenome HGNC:21749
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000303904.8 hg38 chr7 100,088,969 100,092,187 3,219
ENST00000418625.5 hg38 chr7 100,088,981 100,091,905 2,925
ENST00000303904.8 hg19 chr7 99,686,592 99,689,810 3,219
ENST00000418625.5 hg19 chr7 99,686,604 99,689,528 2,925
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